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首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Clinically relevant pain relief with an ibuprofen-releasing foam dressing: Results from a randomized, controlled, double-blind clinical trial in exuding, painful venous leg ulcers
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Clinically relevant pain relief with an ibuprofen-releasing foam dressing: Results from a randomized, controlled, double-blind clinical trial in exuding, painful venous leg ulcers

机译:使用布洛芬释放泡沫敷料可缓解临床相关疼痛:渗出性疼痛性小腿静脉溃疡的随机,对照,双盲临床试验结果

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摘要

The objective of this 6-week, 120-patient, double-blind, randomized, controlled trial was to investigate if a foam dressing with ibuprofen provided clinically relevant pain relief (PAR) for exuding, painful venous leg ulcers in comparison with a similar foam dressing without ibuprofen. Primary outcome parameter was PAR compared with baseline pain during the first 5 days of the investigation. PAR was registered by the patient morning and evening. Main end point was proportion of patients reporting a summed PAR score of at least 50% of the total maximum PAR (i.e., responders) and the corresponding number needed to treat (NNT). Wound-related parameters such as ulcer healing, ulcer area reduction, and peri-ulcer skin condition as well as adverse events were recorded during all 6 weeks of the investigation. PAR was significantly greater in the ibuprofen foam group than the comparator group (p = 0.0438). There were 34% responders in the ibuprofen foam group vs. 19% in the comparator group (NNT = 6.8). When evening data were analyzed separately to evaluate PAR over daytime, NNT was 5.3. Wound healing parameters and adverse events were comparable. In conclusion, in this study, the ibuprofen foam dressing provided clinically relevant PAR for patients with exuding, painful venous ulcers.
机译:这项为期6周,120位患者的双盲,随机,对照试验的目的是调查与相似的泡沫相比,使用布洛芬的泡沫敷料是否能为渗出,疼痛的下肢溃疡提供临床相关的疼痛缓解(PAR)。没有布洛芬的敷料。在研究的前5天中,主要结局参数为PAR与基线疼痛相比。 PAR在患者早晚登记。主要终点是报告总PAR分数至少为总最大PAR的50%的患者比例(即反应者)和相应的治疗所需人数(NNT)。在整个研究的6周中,记录了与伤口相关的参数,例如溃疡愈合,溃疡面积减少,溃疡周围皮肤状况以及不良事件。布洛芬泡沫组的PAR明显高于对照组(p = 0.0438)。布洛芬泡沫组有34%的反应者,对比组有19%的反应者(NNT = 6.8)。当分别分析夜间数据以评估白天的PAR时,NNT为5.3。伤口愈合参数和不良事件相当。总之,在本研究中,布洛芬泡沫敷料为患有渗出性疼痛性静脉溃疡的患者提供了临床相关的PAR。

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